A curated catalogue of human genomic structural variation

Variant Details

Variant: esv3891350

Internal ID

19185746

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr8:15545789..15551953	hg38	UCSC Ensembl
Outer	chr8:15543065..15554099	hg38	UCSC Ensembl
Inner	chr8:15403298..15409462	hg19	UCSC Ensembl
Outer	chr8:15400574..15411608	hg19	UCSC Ensembl
Inner	chr8:15447669..15453833	hg18	UCSC Ensembl
Outer	chr8:15444945..15455979	hg18	UCSC Ensembl

Cytoband

8p22

Allele length

Assembly	Allele length
hg38	11035
hg19	11035
hg18	11035

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

M

Merged Variants

Supporting Variants

essv25787499, essv25778363, essv25797088, essv25781139, essv25799833, essv25799862, essv25799307, essv25797093, essv25801544, essv25798116, essv25787027, essv25798117, essv25797893, essv25800610, essv25796429, essv25796647, essv25787181, essv25781412, essv25784017, essv25779143, essv25800830, essv25798229, essv25778996, essv25797309, essv25785431, essv25784864, essv25800455, essv25784046, essv25785668, essv25779578, essv25793625, essv25779160, essv25800990, essv25801531, essv25778644, essv25801602, essv25779299, essv25786423, essv25786272, essv25797432, essv25786926, essv25785726, essv25782420, essv25784084, essv25778957, essv25799652, essv25782435, essv25799602, essv25784149, essv25783831, essv25780500, essv25783899, essv25796819, essv25784508, essv25783193, essv25781519, essv25779552, essv25783874, essv25778591, essv25785079, essv25786845, essv25800494, essv25783751, essv25785562, essv25797880, essv25785557, essv25785230, essv25797871, essv25781663, essv25784949, essv25784578, essv25799294, essv25779103, essv25787625, essv25783861, essv25797067, essv25784876, essv25796876, essv25796339, essv25797939, essv25783153, essv25778763, essv25782978, essv25797108, essv25796545, essv25782810, essv25782744, essv25801071, essv25796047, essv25784808, essv25799285, essv25796711, essv25801075, essv25799071, essv25785008, essv25799146, essv25801646, essv25801304, essv25783622, essv25780782, essv25779277, essv25800243, essv25800057, essv25783452, essv25782926, essv25786584, essv25800071, essv25783211, essv25796452, essv25786226, essv25797495, essv25787284, essv25783044, essv25797305, essv25784813, essv25796053, essv25785178, essv25799556, essv25785665, essv25783756, essv25779406, essv25778230, essv25800738, essv25780015, essv25801378, essv25784376, essv25800024, essv25780301, essv25797104, essv25785211, essv25779888, essv25799368, essv25778408, essv25784093, essv25783797, essv25797472, essv25786974, essv25785600, essv25785239, essv25797401, essv25800933, essv25787237, essv25796279, essv25783842, essv25781969, essv25796188, essv25781724, essv25779061, essv25794777, essv25781596, essv25796334, essv25796799, essv25801517, essv25796387, essv25786936, essv25783959, essv25798182, essv25796701, essv25800309, essv25797737, essv25796846, essv25785496, essv25784870, essv25786163, essv25780821, essv25800854, essv25798931, essv25797164, essv25778942, essv25796966, essv25781800, essv25780883, essv25783870, essv25796622, essv25782065, essv25797787, essv25796587, essv25800372, essv25800009, essv25784142, essv25778554, essv25801110, essv25797835, essv25784367, essv25796653, essv25797074, essv25783603, essv25783776, essv25780168, essv25783060, essv25781882, essv25800921, essv25785283, essv25783138, essv25799507, essv25798083, essv25797557, essv25780106, essv25779835, essv25801118, essv25801199, essv25782387, essv25801001, essv25782940, essv25781667, essv25799051, essv25801638, essv25778488, essv25797563, essv25795254, essv25785378, essv25800939, essv25800431, essv25791014, essv25779489

Samples

Known Genes

Method

SNP array

Analysis

Platform

Illumina HumanHap 610
Illumina Human OmniExpress

Comments

Reference

Suktitipat_et_al_2014

Pubmed ID

Accession Number(s)

Frequency

Sample Size	3017
Observed Gain	0
Observed Loss	215
Observed Complex	0
Frequency	n/a